Role & responsibilities

1. Giving stage wise line clearance in Tablet manufacturing department covering all the

sections like granulations, compression and coating.

2. Responsible for monitoring the In-process quality control checks in Tablet manufacturing department.

3. Comparing the appearance of coated tablets for all products against the standards.

4. Collection of samples stage wise for analysis including Residual solvent samples and

handover for QC Testing.

5. Checking any OOS recorded during online process and reporting to seniors.

6. Final BMR reconciliation before release for next process/packing.

7. Compilation of all Tablets IPQC datas in system.

8. Clearance of activities in tablets during shift operations.

9. Any other jobs & responsibility as and when entrusted by Head of the department.

10.



Line clearance at every stage of Manufacturing of Tablets & Granules and sign the respective documents.

11. To stop the line in case of any major non-compliance and with proper approval and guidance from seniors and Head of the department.

12. To reconcile the BMR online and handover the final completed BMR to packing dept. for further process.

Preferred candidate profile

Education- B.Pharma/M.Pharma

Experience - 1 to 3 Years (Pharmaceutical Industry only)

Location- Peenya, Bangalore

Perks and advantages

Regards,

Divya S

(Email Id.- [email protected] & Mob. No.- (phone hidden))

📌 Jr. Executive- QA (Bengaluru)
🏢 Meyer Organics
📍 Bengaluru